GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Flavobacterium beibuense F44-8

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_035130203.1 Q763_RS01195 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_000769915.1:WP_035130203.1
          Length = 317

 Score =  294 bits (752), Expect = 2e-84
 Identities = 156/317 (49%), Positives = 216/317 (68%), Gaps = 16/317 (5%)

Query: 8   RVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPALME 67
           + +I+GSGPAGY+AA+YAARA++ P++ TGM+ GGQLTTTTEVDN+PG   G+ GP +M 
Sbjct: 9   KCLIIGSGPAGYTAAIYAARADMNPVIYTGMEPGGQLTTTTEVDNFPGYPEGIDGPTMMV 68

Query: 68  RMREHAERFETEIVFDHINAVDFAAK-----PYTLTGDSATYTCDALIIATGASARYLGL 122
           ++++ AERF TE+    + A++ + +       T+  +   +    +II+TGA+A+YLGL
Sbjct: 69  QLQQQAERFGTEVRIGMVTAIELSKEHGGWHKATIDNNKEVHA-QTVIISTGATAKYLGL 127

Query: 123 PSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFR 182
           PSE+   G GVSACA CDGFFYR + VA+VG G+TA EEA YLANI   VT++ R++  R
Sbjct: 128 PSEQRLRGGGVSACAVCDGFFYRGQDVAIVGAGDTAAEEATYLANICKNVTMLVRKDFMR 187

Query: 183 AEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNND-GSFDELKVDGVFIA 241
           A K +  ++        + +  N  +DEVLG+ + V G R  NN  G   E+ V G+FIA
Sbjct: 188 ASKAMQHRVE---NTPNLTVLYNTEVDEVLGEQV-VEGLRTVNNQTGEKTEIPVTGLFIA 243

Query: 242 IGHTPNTSLFEGQLTLKD-GYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGA 300
           IGH PNT +F+GQL + + GYL+ Q    G +T T++ G+FA+GDV D  YRQAIT+AG+
Sbjct: 244 IGHKPNTDIFKGQLDMDETGYLITQ----GKSTKTNLPGVFASGDVQDKEYRQAITAAGS 299

Query: 301 GCMAALDTERYLDGLQN 317
           GCMAALD ERYL  L N
Sbjct: 300 GCMAALDAERYLATLDN 316


Lambda     K      H
   0.318    0.135    0.386 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 300
Number of extensions: 14
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 320
Length of database: 317
Length adjustment: 27
Effective length of query: 293
Effective length of database: 290
Effective search space:    84970
Effective search space used:    84970
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory